The following data is part of a premarket notification filed by Carefusion with the FDA for Pleurx Pleural Catheter System.
Device ID | K160450 |
510k Number | K160450 |
Device Name: | Pleurx Pleural Catheter System |
Classification | Apparatus, Suction, Patient Care |
Applicant | CAREFUSION 75 NORTH FAIRWAY DRIVE Vernon Hills, IL 60061 |
Contact | Joy Greidanus |
Correspondent | Tamara A. Brey CAREFUSION 75 NORTH FAIRWAY DRIVE Vernon Hills, IL 60061 |
Product Code | DWM |
CFR Regulation Number | 870.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-18 |
Decision Date | 2016-10-31 |
Summary: | summary |